FS SERIES WHEELCHAIR
K-Number: K041814 · 2004-07-20
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Device Summary
Frequently Asked Questions
What is the FS SERIES WHEELCHAIR?
FS SERIES WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2004-07-20. The listed applicant is Foshan Dongfang Medical Equipment Manufactory(Ltd). The 510(k) number is K041814.
When did FS SERIES WHEELCHAIR receive FDA 510(k) clearance?
FS SERIES WHEELCHAIR received FDA 510(k) clearance on 2004-07-20, under 510(k) number K041814.
Who is the listed applicant for FS SERIES WHEELCHAIR?
The FDA 510(k) record lists Foshan Dongfang Medical Equipment Manufactory(Ltd) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FS SERIES WHEELCHAIR?
The FDA product code for FS SERIES WHEELCHAIR is IOR.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: IOR)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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